Canonical Allele Identifier: CA2611201227

Gene: FGFR2

Linked Data

• gnomAD v4: 10-121520212-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121520217_121520218del , CM000672.2:g.121520217_121520218del	GRCh38
NC_000010.10:g.123279731_123279732del , CM000672.1:g.123279731_123279732del	GRCh37
NC_000010.9:g.123269721_123269722del	NCBI36
NG_012449.1:g.83245_83246del
NG_012449.2:g.83245_83246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.749-45_749-44del MANE Plus Clinical	ENSP00000410294.2:n.749-45_749-44del
ENST00000351936.11:c.749-45_749-44del	ENSP00000309878.10:n.749-45_749-44del
ENST00000638709.2:c.-422-45_-422-44del	ENSP00000491912.2:n.-422-45_-422-44del
ENST00000682296.1:n.97-45_97-44del
ENST00000682400.1:n.404-45_404-44del
ENST00000682550.1:c.404-45_404-44del	ENSP00000507633.1:n.404-45_404-44del
ENST00000682772.1:c.-422-45_-422-44del	ENSP00000506848.1:n.-422-45_-422-44del
ENST00000683211.1:c.749-45_749-44del	ENSP00000508257.1:n.749-45_749-44del
ENST00000683250.1:c.404-16273_404-16272del	ENSP00000506847.1:n.404-16273_404-16272del
ENST00000683418.1:n.3096-45_3096-44del
ENST00000683678.1:n.749-45_749-44del
ENST00000684153.1:c.404-45_404-44del	ENSP00000506937.1:n.404-45_404-44del
ENST00000358487.10:c.749-45_749-44del MANE Select	ENSP00000351276.6:n.749-45_749-44del
ENST00000336553.10:c.482-45_482-44del	ENSP00000337665.6:n.482-45_482-44del
ENST00000346997.6:c.749-45_749-44del	ENSP00000263451.5:n.749-45_749-44del
ENST00000351936.10:c.749-45_749-44del	ENSP00000309878.9:n.749-45_749-44del
ENST00000356226.8:c.404-45_404-44del	ENSP00000348559.4:n.404-45_404-44del
ENST00000357555.9:c.482-45_482-44del	ENSP00000350166.5:n.482-45_482-44del
ENST00000358487.9:c.749-45_749-44del	ENSP00000351276.5:n.749-45_749-44del
ENST00000360144.7:c.482-45_482-44del	ENSP00000353262.3:n.482-45_482-44del
ENST00000369056.5:c.749-45_749-44del	ENSP00000358052.1:n.749-45_749-44del
ENST00000369058.7:c.749-45_749-44del	ENSP00000358054.3:n.749-45_749-44del
ENST00000369059.5:c.404-45_404-44del	ENSP00000358055.1:n.404-45_404-44del
ENST00000369060.8:c.749-45_749-44del	ENSP00000358056.4:n.749-45_749-44del
ENST00000369061.8:c.749-4895_749-4894del	ENSP00000358057.4:n.749-4895_749-4894del
ENST00000457416.6:c.749-45_749-44del	ENSP00000410294.2:n.749-45_749-44del
ENST00000478859.5:c.65-45_65-44del	ENSP00000474011.1:n.65-45_65-44del
ENST00000490349.5:n.1010-45_1010-44del
ENST00000604236.5:c.404-45_404-44del	ENSP00000474109.1:n.404-45_404-44del
ENST00000613048.4:c.482-45_482-44del	ENSP00000484154.1:n.482-45_482-44del
NM_000141.4:c.749-45_749-44del	NP_000132.3:n.749-45_749-44del
NM_001144913.1:c.749-45_749-44del	NP_001138385.1:n.749-45_749-44del
NM_001144914.1:c.749-4895_749-4894del	NP_001138386.1:n.749-4895_749-4894del
NM_001144915.1:c.482-45_482-44del	NP_001138387.1:n.482-45_482-44del
NM_001144916.1:c.404-45_404-44del	NP_001138388.1:n.404-45_404-44del
NM_001144917.1:c.749-45_749-44del	NP_001138389.1:n.749-45_749-44del
NM_001144918.1:c.404-45_404-44del	NP_001138390.1:n.404-45_404-44del
NM_001144919.1:c.482-45_482-44del	NP_001138391.1:n.482-45_482-44del
NM_022970.3:c.749-45_749-44del	NP_075259.4:n.749-45_749-44del
NM_023029.2:c.482-45_482-44del	NP_075418.1:n.482-45_482-44del
NR_073009.1:n.1051-45_1051-44del
XM_006717708.2:c.806-45_806-44del	XP_006717771.1:n.806-45_806-44del
XM_006717709.2:c.806-45_806-44del	XP_006717772.1:n.806-45_806-44del
XM_006717710.2:c.806-45_806-44del	XP_006717773.1:n.806-45_806-44del
XM_006717711.2:c.539-45_539-44del	XP_006717774.1:n.539-45_539-44del
XM_006717712.2:c.461-45_461-44del	XP_006717775.1:n.461-45_461-44del
XM_006717713.2:c.806-45_806-44del	XP_006717776.1:n.806-45_806-44del
XM_011539510.1:c.65-45_65-44del	XP_011537812.1:n.65-45_65-44del
NM_001320654.1:c.65-45_65-44del	NP_001307583.1:n.65-45_65-44del
NM_001320658.1:c.749-45_749-44del	NP_001307587.1:n.749-45_749-44del
XM_006717708.3:c.806-45_806-44del	XP_006717771.1:n.806-45_806-44del
XM_006717710.4:c.806-45_806-44del	XP_006717773.1:n.806-45_806-44del
XM_017015920.2:c.806-45_806-44del	XP_016871409.1:n.806-45_806-44del
XM_017015921.2:c.806-45_806-44del	XP_016871410.1:n.806-45_806-44del
XM_017015924.2:c.461-45_461-44del	XP_016871413.1:n.461-45_461-44del
XM_017015925.2:c.461-45_461-44del	XP_016871414.1:n.461-45_461-44del
XM_024447887.1:c.539-45_539-44del	XP_024303655.1:n.539-45_539-44del
XM_024447888.1:c.539-45_539-44del	XP_024303656.1:n.539-45_539-44del
XM_024447889.1:c.539-45_539-44del	XP_024303657.1:n.539-45_539-44del
XM_024447890.1:c.539-45_539-44del	XP_024303658.1:n.539-45_539-44del
XM_024447891.1:c.461-45_461-44del	XP_024303659.1:n.461-45_461-44del
XM_024447892.1:c.-422-45_-422-44del	XP_024303660.1:n.-422-45_-422-44del
NM_000141.5:c.749-45_749-44del MANE Select	NP_000132.3:n.749-45_749-44del
NM_001144917.2:c.749-45_749-44del	NP_001138389.1:n.749-45_749-44del
NM_001144918.2:c.404-45_404-44del	NP_001138390.1:n.404-45_404-44del
NM_001144919.2:c.482-45_482-44del	NP_001138391.1:n.482-45_482-44del
NM_001320658.2:c.749-45_749-44del	NP_001307587.1:n.749-45_749-44del
NR_073009.2:n.1037-45_1037-44del
NM_001144915.2:c.482-45_482-44del	NP_001138387.1:n.482-45_482-44del
NM_001144916.2:c.404-45_404-44del	NP_001138388.1:n.404-45_404-44del
NM_001320654.2:c.65-45_65-44del	NP_001307583.1:n.65-45_65-44del